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Total synthesis of (+/-)-crinine via the regioselective stille coupling and Diels-Alder reaction of 3,5-dibromo-2-pyrone

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dc.contributor.authorTam, Nguyen Thanh-
dc.contributor.authorCho, Cheon-Gyu-
dc.date.accessioned2022-12-21T04:42:11Z-
dc.date.available2022-12-21T04:42:11Z-
dc.date.created2022-08-26-
dc.date.issued2008-02-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/179038-
dc.description.abstractThe regioselective synthesis and Diels-Alder cycloaddition of 3-(3,4-methylenedioxyphenyl)-5-bromo-2-pyrone provided a new synthetic route to crinine. The vinyl bromide group can be used as a handle for further derivatization.-
dc.language영어-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.titleTotal synthesis of (+/-)-crinine via the regioselective stille coupling and Diels-Alder reaction of 3,5-dibromo-2-pyrone-
dc.typeArticle-
dc.contributor.affiliatedAuthorCho, Cheon-Gyu-
dc.identifier.doi10.1021/ol702907u-
dc.identifier.scopusid2-s2.0-39749187155-
dc.identifier.wosid000252989500020-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.10, no.4, pp.601 - 603-
dc.relation.isPartOfORGANIC LETTERS-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume10-
dc.citation.number4-
dc.citation.startPage601-
dc.citation.endPage603-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusAMARYLLIDACEAE ALKALOIDS-
dc.subject.keywordPlusCYCLOADDITIONS-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/ol702907u-
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